posted on 2018-10-03, 00:00authored byAllen
F. Brooks, Lindsey R. Drake, Xia Shao, Austin Zhao, Peter J. H. Scott, Michael R. Kilbourn
The development of
a positron emission tomography (PET)/magnetic
resonance spectroscopy (MRS) hybrid imaging agent allows for functional
imaging by both methods with a single imaging agent. Enzyme substrates
that are cleaved to form two metabolites present an interesting opportunity,
as the unique metabolites generated might each be detected by a different
modality. To be successful, such enzyme substrates would require administration
of doses that (a) reach the in vivo target tissue
at concentrations necessary for MRS imaging, (b) do not show substrate
inhibition of tissue uptake or enzymatic activity, and (c) provide
PET images that still reflect the action of the enzyme. We report in vitro and in vivo proof-of-concept studies
of a carbon-11 small molecule substrate for brain monoamine oxidases
that, upon enzyme-mediated cleavage, produces two metabolites, one
detectable by PET and the other by MRS.